RecallRadar
ModerateReported May 27, 2026 (5 weeks ago)

Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement Oral L…

Recalled by Safecor Health, LLC

Drug recall

Safecor Health, LLC

Class II — moderate

Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Safecor Health, LLC has recalled Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement Oral L…, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on May 27, 2026 and was initiated on May 1, 2026. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement Oral L…, with approximately 520 syringes affected. The company behind the recall is Safecor Health, LLC, based in Columbus, OH. The FDA describes the product as: “Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement Oral Liquid, Contains: Folic Acid 799 mcg/5mL, Delivers 5 mL per oral syringe, (Nephronex), Mfg By: LLORENS; Pkg by: Safecor, Columbus, OH. NDC 54859-0516-08”

Why was Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement Oral L… recalled?

According to the FDA, the stated reason for the recall is: “Presence of a Foreign Substance; black particles observed in liquid.”

What should you do?

If you think you may have bought Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement Oral L…, compare it against the product description and identifying codes (Lot, expiry: Lots 26110722, 26110743, exp 9/8/2026; Lot 26111218, exp 9/9/2026) before using it. This recall is currently listed as ongoing.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Safecor Health, LLC or your local health authority.

About this recall

This recall was distributed in OH. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.

Full recall details

Status
Ongoing
Date reported
May 27, 2026
Recall started
May 1, 2026
Distributed in
OH
What was recalled
Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement Oral Liquid, Contains: Folic Acid 799 mcg/5mL, Delivers 5 mL per oral syringe, (Nephronex), Mfg By: LLORENS; Pkg by: Safecor, Columbus, OH. NDC 54859-0516-08
Why it was recalled (as stated by the FDA)
Presence of a Foreign Substance; black particles observed in liquid
How to identify the affected product
Lot, expiry: Lots 26110722, 26110743, exp 9/8/2026; Lot 26111218, exp 9/9/2026
Amount recalled
520 syringes

What you can do

Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.

Quick answers

Why was Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement Oral L… recalled?+

According to the FDA: Presence of a Foreign Substance;

How serious is this recall?+

Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

What should I do if I have Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement Oral L…?+

Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: D-0549-2026. Information last synced from the FDA on July 5, 2026.

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